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91.
中国某些野生和栽培茶的核型研究 总被引:9,自引:0,他引:9
研究了茶的4个变种和广东野生毛叶茶等共12个材料的核型。所有材料的染色体数目均是2n=30,为二倍体。所有中国大叶变种(越南大叶除外)(Cametlia sinensis var. macrophylla)和阿萨姆大叶变种(C. sinensis var. assamica)均具比较对称或原始的“2A”核型;中国小叶变种(C.sinensis var.bohea)(“铁观音”品种除外),掸部变种(C.sinensis var. shan form)和广东野生毛叶茶(C. ptilophylla)均具较不对称或较进化的“2B”核型。根据核型特征,植物习性和地理分布,作者认为中国四川和云南可能是茶的起源中心,向东或北迁移,演变为中国小叶变种;向南移则演变为阿萨姆变种和掸部变种。 相似文献
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Teresa de Sa E Melo Patrice Morlière Sonia Goldstein René Santus Louis Dubertret Dominique Lagrange 《Biochemical and biophysical research communications》1984,120(2):670-676
5-methoxypsoralen (5-MOP) binds to human serum low density lipoproteins (LDL) according to a two-step process. Scatchard analysis of the first step yields K = 1.4 × 105 M?1 and 4 binding sites. It involves the LDL apoprotein. The second step corresponds to a solubilization, in the lipidic core, of ? 45 molecules of 5MOP per LDL molecule. It is accompanied by a large blue shift of the 5MOP fluorescence. The ability of LDL to bind 5MOP and to carry it into various cells may explain some biological effects sometimes encountered during PUVA therapy. 相似文献
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A numerical algorithm has been developed for the estimation of the mechanical parameters of the human respiratory system. In order to estimate the pulmonary resistance and the dynamic pulmonary elastance, the transpulmonary pressure and the airflow at the mouth or nose are expanded in Chebyshev series. The nonlinear mathematical lung model and a set of measurements for airflow and pressure are then handled by the numerical technique. The lung model includes a component to account for turbulent flow in the larynx and trachea. This contribution presents an alternative method for lung parameter estimation and differs from most existing methods in that it does not need measurements for the tidal volume. It therefore eliminates the use of a body plethysmograph. The method may also find potential application to various other parameter identification problems. 相似文献
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Spores of Nosema bombycis derived from diseased insects were highly purified by Urografin density gradient centrifugation. Antheraea eucalypti cells were inoculated with the purified spores primed with 0.1 n KOH solution to start a continuous propagation of N. bombycis in cell culture. The first increase in the number of infected A. eucalypti cells was observed at 48 hr postinoculation, and it was caused by the secondary infective forms of N. bombycis. The secondary infective forms were produced during the course of sporoblast differentiation. The parasites in cell cultures divided synchronously until 36 hr postinoculation. Mature spores were observed initially 6 days postinoculation at 27°C. The infected cultures were subcultured extensively for more than 1 year with the addition of healthy A. eucalypti cells. 相似文献
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